Tigroid pattern on magnetic resonance imaging in Lowe syndrome

Journal of Clinical Neuroscience

Volumn 16, Issue 1, 2009, Pages 112-114

  Onur, Mehmet Ruhi ^a   Senol, Utku ^b   Mihçi, Ercan ^b   Lüleci, Ersin ^b  

^a Kovancilar Government Hospital   (Turkey)

^b AKDENIZ UNIVERSITY FACULTY OF MEDICINE   (Turkey)

Author keywords

Lowe syndrome; MRI; Oculocerebrorenal syndrome

Indexed keywords

AMINOACIDURIA; ARTICLE; CAMPTODACTYLY; CASE REPORT; CATARACT; CLINICAL FEATURE; CONGENITAL MALFORMATION; CONGENITAL NYSTAGMUS; CRYPTORCHISM; DIAGNOSTIC IMAGING; ENOPHTHALMOS; FOLLOW UP; HUMAN; KIDNEY TUBULE ABSORPTION; LOWE SYNDROME; MALE; MUSCLE HYPOTONIA; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PHOSPHATURIA; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; URINALYSIS; WHITE MATTER;

HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; OCULOCEREBRORENAL SYNDROME;

EID: 56949083217     PISSN: 09675868     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jocn.2008.02.011     Document Type: Article

References (12)

1. Lowe C., Terrey M., and Mc Lachlan E.A. Organic aciduria, decreased renal ammonia production, hydrophtalmos and mental retardation: A clinical entity. Am J Dis Child 83 (1952) 164-184
2. O'Tauma D.A., and Lasker D.W. Oculocerebrorenal syndrome: case report with CT and MR correlates. AJNR 8 (1987) 555-557
3. Charnas L., Bernar J., Pezeshkpour G.H., et al. MRI findings and peripheral neuropathy in Lowe's syndrome. Neuropediatrics 19 (1988) 7-9
4. Gabrielli O., Salvolini U., Copa G.V., et al. Magnetic resonance imaging in the malformative syndromes with mental retardation. Pediatr Radiol 21 (1990) 16-19
5. Atree O., Olivos I.M., Okabe I., et al. The Lowe oculocerebrorenal syndrome gene encodes a novel protein highly homologous to inositol polyphosphate-5-phosphatase. Nature 358 (1992) 239-242
6. Ungewickell A.J., and Majerus P.W. Increased levels of plasma lysosomal enzymes in patients with Lowe syndrome. PNAS 96 (1999) 13342-13344
7. Schneider J.F., Boltshauser E., Neuhaus T.J., et al. MRI and proton spectroscopy in Lowe syndrome. Neuropediatrics 1 (2001) 45-48
8. Cheon J.E., Kim I.O., Hwang Y.S., et al. Leucodystrophy in children: A pictorial review of MR imaging features. Radiographics 22 (2002) 461-476
9. Caro P.A., and Marks H.G. Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher disease. Magn Reson Imaging 8 (1990) 791-796
10. Scheffer I.E., Baraitser M., Wilson J., et al. Pelizaeus-Merzbacher disease: Classical or connatal?. Neuropediatrics 22 (1991) 71-78
11. Sener R.N. Diffusion magnetic resonance imaging patterns in metabolic and toxic brain disorders. Acta Radiol 45 (2004) 561-570
12. Carroll W.J., Woodruff W.W., and Camdan T.E. MR findings in oculocerebrorenal syndrome. AJNR 14 (1993) 449-451